Biofilm-producing and specific antibiotic resistance genes in Pseudomonas aeruginosa isolated from patients admitted to a tertiary care hospital, Bangladesh

IF 1.5 Q4 INFECTIOUS DISEASES
Rubaiya Binte Kabir , Tasnim Ahsan , Md. Faizur Rahman , Mohammad Jobayer , SM Shamsuzzaman
{"title":"Biofilm-producing and specific antibiotic resistance genes in Pseudomonas aeruginosa isolated from patients admitted to a tertiary care hospital, Bangladesh","authors":"Rubaiya Binte Kabir ,&nbsp;Tasnim Ahsan ,&nbsp;Md. Faizur Rahman ,&nbsp;Mohammad Jobayer ,&nbsp;SM Shamsuzzaman","doi":"10.1016/j.ijregi.2024.100369","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><p>Biofilms are responsible for persistent infections and antimicrobial resistance<em>. Pseudomonas aeruginosa</em> was investigated with its ability to form biofilm by detecting genes responsible for producing biofilms and biofilm-specific antimicrobial resistance. The association between antibiotic resistance and biofilm was investigated.</p></div><div><h3>Methods</h3><p>This cross-sectional study was conducted from July 2017 to December 2018. A total of 446 samples (infected burn, surgical wounds, and endotracheal aspirate) were collected from admitted patients of Dhaka Medical College and Hospital, Bangladesh. <em>P. aeruginosa</em> was isolated and identified by biochemical tests and polymerase chain reaction. Biofilm production by tissue culture plate method followed by detection of biofilm-producing genes (<em>pqsA, pslA, pslD, pslH, pelA, lasR</em>) and biofilm-specific antibiotic resistance genes (<em>ndvB</em>, PA1874, PA1876, PA1877) by polymerase chain reaction were done. Antibiotic susceptibility test was carried out by disk diffusion method; for colistin agar dilution method of minimal inhibitory concentration was followed.</p></div><div><h3>Results</h3><p>Among 232 (52.02%) positive strains of <em>P. aeruginosa</em>, 24 (10.30%) produced biofilms in tissue culture plate. Among biofilm-producing genes, <em>pqsA</em> was the highest (79.17%). <em>pslA</em> and <em>pelA</em> were 70.83%<em>, pslD</em> 45.83%, <em>pslH</em> and <em>lasR</em> 37.5%. Among biofilm-specific antibiotic resistance genes, 16.67% were <em>ndvB</em>, and 8.33% were PA1874 and PA1877. Biofilm-forming strains were significantly resistant to colistin.</p></div><div><h3>Conclusions</h3><p>Detection of biofilm-forming genes may be a good tool for the evaluation of biofilm production, which will help in prompt and better management of chronic or device-associated infections.</p></div>","PeriodicalId":73335,"journal":{"name":"IJID regions","volume":null,"pages":null},"PeriodicalIF":1.5000,"publicationDate":"2024-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772707624000407/pdfft?md5=2047b17b95f79ae5bf420e32de614b78&pid=1-s2.0-S2772707624000407-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IJID regions","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772707624000407","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives

Biofilms are responsible for persistent infections and antimicrobial resistance. Pseudomonas aeruginosa was investigated with its ability to form biofilm by detecting genes responsible for producing biofilms and biofilm-specific antimicrobial resistance. The association between antibiotic resistance and biofilm was investigated.

Methods

This cross-sectional study was conducted from July 2017 to December 2018. A total of 446 samples (infected burn, surgical wounds, and endotracheal aspirate) were collected from admitted patients of Dhaka Medical College and Hospital, Bangladesh. P. aeruginosa was isolated and identified by biochemical tests and polymerase chain reaction. Biofilm production by tissue culture plate method followed by detection of biofilm-producing genes (pqsA, pslA, pslD, pslH, pelA, lasR) and biofilm-specific antibiotic resistance genes (ndvB, PA1874, PA1876, PA1877) by polymerase chain reaction were done. Antibiotic susceptibility test was carried out by disk diffusion method; for colistin agar dilution method of minimal inhibitory concentration was followed.

Results

Among 232 (52.02%) positive strains of P. aeruginosa, 24 (10.30%) produced biofilms in tissue culture plate. Among biofilm-producing genes, pqsA was the highest (79.17%). pslA and pelA were 70.83%, pslD 45.83%, pslH and lasR 37.5%. Among biofilm-specific antibiotic resistance genes, 16.67% were ndvB, and 8.33% were PA1874 and PA1877. Biofilm-forming strains were significantly resistant to colistin.

Conclusions

Detection of biofilm-forming genes may be a good tool for the evaluation of biofilm production, which will help in prompt and better management of chronic or device-associated infections.

从孟加拉国一家三甲医院住院病人体内分离的铜绿假单胞菌的生物膜产生基因和特异性抗生素耐药性基因
目的 生物膜是造成持续感染和抗菌药耐药性的原因。通过检测产生生物膜的基因和生物膜特异性抗菌药耐药性,研究铜绿假单胞菌形成生物膜的能力。方法这项横断面研究于 2017 年 7 月至 2018 年 12 月进行。共收集了 446 份样本(感染性烧伤、手术伤口和气管内吸出物),均来自孟加拉国达卡医学院和医院的住院患者。通过生化测试和聚合酶链反应分离并鉴定了铜绿假单胞菌。采用组织培养平板法产生生物膜,然后通过聚合酶链反应检测生物膜产生基因(pssA、pslA、pslD、pslH、pelA、rasR)和生物膜特异性抗生素耐药基因(ndvB、PA1874、PA1876、PA1877)。结果 在 232 株(52.02%)铜绿假单胞菌阳性菌株中,有 24 株(10.30%)在组织培养板中产生了生物膜。在产生生物膜的基因中,pqsA最高(79.17%),pslA和pelA占70.83%,pslD占45.83%,pslH和lasR占37.5%。在生物膜特异性抗生素耐药基因中,ndvB 占 16.67%,PA1874 和 PA1877 占 8.33%。结论检测生物膜形成基因可能是评估生物膜产生的一个很好的工具,有助于及时、更好地处理慢性或器械相关感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
IJID regions
IJID regions Infectious Diseases
CiteScore
1.60
自引率
0.00%
发文量
0
审稿时长
64 days
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信